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Dystrophin antibody (AA 114-263)

This Mouse Monoclonal antibody specifically detects Dystrophin in ELISA and IHC (p). It exhibits reactivity toward Human.
Catalog No. ABIN7870169
$640.46
Plus shipping costs $50.00
100 μg
Shipping to: United States
Delivery in 2 to 4 Business Days

Quick Overview for Dystrophin antibody (AA 114-263) (ABIN7870169)

Target

See all Dystrophin (DMD) Antibodies
Dystrophin (DMD)

Reactivity

  • 112
  • 18
  • 17
  • 3
  • 2
Human

Host

  • 74
  • 39
Mouse

Clonality

  • 88
  • 25
Monoclonal

Conjugate

  • 68
  • 5
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
This Dystrophin antibody is un-conjugated

Application

  • 57
  • 32
  • 29
  • 27
  • 26
  • 12
  • 10
  • 8
  • 4
  • 2
  • 2
  • 1
  • 1
ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Grade

Carrier-free

Clone

DMD-3676
  • Binding Specificity

    • 55
    • 8
    • 6
    • 6
    • 4
    • 4
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 114-263

    Purpose

    DMD Antibody / Dystrophin (azide and preservative free)

    Purification

    Protein A/G affinity

    Immunogen

    A portion of amino acids 114-263 from the human protein was used as the immunogen for the DMD antibody.

    Isotype

    IgG2b, kappa
  • Application Notes

    Optimal dilution of the DMD antibody should be determined by the researcher.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 mg/mL

    Buffer

    1 mg/mL in 1X PBS, BSA free, sodium azide free

    Preservative

    Azide free

    Storage

    -20 °C

    Storage Comment

    Aliquot the DMD antibody and store frozen at -20oC or colder. Avoid repeated freeze-thaw cycles.
  • Target

    Dystrophin (DMD)

    Alternative Name

    DMD

    Background

    Dystrophin-glycoprotein complex (DGC) connects the F-Actin cytoskeleton on the inner surface of muscle fibers to the surrounding extracellular matrix, through the cell membrane interface. A deficiency in this protein contributes to Duchenne (DMD) and Becker (BMD) muscular dystrophies. The human dystrophin gene measures 2.4 megabases, has more than 80 exons, produces a 14 kb mRNA and contains at least 8 independent tissue-specific promoters and 2 poly A sites. The dystrophin mRNA can undergo differential splicing and produce a range of transcripts that encode a large set of proteins. Dystrophin represents approximately 0.002 % of total striated muscle protein and localizes to triadic junctions in skeletal muscle, where it is thought to influence calcium ion homeostasis and force transmission.

    UniProt

    P11532

    Pathways

    Skeletal Muscle Fiber Development
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